The influence of the tumor immune microenvironment by the glycolytic process still remains undefined; our analysis revealed that the infiltration of B cells, mast cells, monocytes, plasma cells, activated NK cells, memory CD4+ T cells, and CD8+ T cells was significantly increased in the low-risk group, while resting NK cell infiltration was positively correlated with the risk score. This evidence concerns the gene CD4 and neoplasm.